This page is still under development!! But in the mean time you could check out this little bit of information we have for GPs.
What do GP’s need to know about FragileX?
Fragile X is associate with inherited genetic changes in the Fragile X gene. A referral for genetic testing is required for diagnosis. The gene (also known by its scientific name of “FMR1”) can be normal, but it can also exhibit a “premutation” or a “full mutation”. When a premutation or full mutation is present, it can result in a Fragile X condition….